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Fine-scale structural variation of the human genome

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Figure

Figure 1 Detection of structural variation. (a) The underlying paired-end sequence methodology used to detect structural variation
Table 1 Summary of structural variants determined by paired-end sequence analysis
Figure 4 Genotyping analysis of structural variants. PCR validation and genotyping for seven insertion-deletion sites identified in fully sequenced fosmids, confirming (a) an 8.2-kb deletion in fosmid 3777M04, (b) a 13.3-kb deletion in fosmid 2588B13, (c)

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